Chemically polished polycrystalline alumina material

ABSTRACT

Increased optical transmission is provided for a body of light transmissive polycrystalline alumina body treated at elevated temperatures with a molten flux composition. A tube of the flux polished material which can be used as the light transmissive envelope for high intensity discharge lamps especially sodium vapor lamps, improves light output from the lamp as the result of increased in-line transmission for the treated envelope member. A method of chemically polishing polycrystalline alumina material in this manner is also disclosed.

BACKGROUND OF THE INVENTION

The present invention relates to a transmissive body of high densitypolycrystalline alumina wherein the major surfaces have been polishedwith a molten fluxing agent to provide increased optical transmission. Atubular form of the flux polished material when used as the lighttransmissive envelope for an improved high intensity electric dischargelamp provides higher light-output than can be generally obtained withunpolished alumina material. The improved envelope material isparticularly useful in high intensity sodium vapor lamp constructions ofthe type utilizing self heated electrodes, that is electrodes heated bythe discharge and not by current from an external source.

High intensity sodium vapor lamps of the kind described in U.S. Pat. No.3,248,590 - Schmidt, entitled "High Pressure Sodium Vapor Lamp," requirethe above type electrodes. These lamps further employ a slender tubularenvelope of lighttransmissive, high density, polycrystalline aluminamaterial which is resistant to sodium at high temperatures. Aparticularly suitable high purity alumina of this type is describedalong with methods for its preparation in a U.S. Pat. No. 3,026,210 -Coble wherein said material exhibits an in-line transmission of not lessthan 0.5% per millimeter thickness of the tube for radiant energy of allwavelengths in the wavelength region from about 0.3 micron to about 6.6microns with an in-line transmission of not less than 10% at somewavelength within said wavelength range. Such polycrystalline aluminamaterial generally contains a small but effective amount up to 0.5weight percent magnesia to provide optical transparency wherein themagnesia content can be present primarily as an alumina-magnesia spinel.The filling in such high intensity sodium vapor lamps comprises sodiumalong with a rare gas such as xenon to facilitate starting and mercuryfor improved efficiency. Both ends of the alumina tube are sealed byrefractory metal closure members, suitably niobium end caps bonded tothe alumina tube with a glassy sealing material. Each end cap supportsan electrode extending along the axis of the tube such as a tungsten rodhaving a double coil of tungsten wire wound around its inner end andwith the electrodes further being coated with a suitable electronemissive material. A lamp of this construction is further described in aU.S. Pat. No. 3,708,710 - Smyser et al, along with a suitable method oflamp fabrication, so that it becomes unnecessary to repeat such detailsin the present specification.

It is also known to chemically polish opaque polycrystalline aluminaobjects in a fused borax bath so that dislocations and grain boundariesare not preferentially etched. The observed effect with this techniquewas a smooth and highly reflective surface being produced on the aluminamaterial. Improved mechanical strength resulted from such treatmentwhich is described in the technical article entitled "Chemical Polishand Strength of Alumina", by A. G. King, published in Vol.3, MaterialsScience Research (1966).

SUMMARY OF THE INVENTION

It has now been found, surprisingly, that optical transmission of alight transmissive polycrystalline alumina material as described in theaforementioned U.S. Pat. No. 3,026,210 Patent is also significantlyincreased by a flux polishing treatment and to such a degree that lightoutput characteristics of high intensity electric discharge lampsutilizing the polished arc chambers are improved. The improvementthereby obtained in light-output for such lamps has been found superiorcompared with the same lamp using an arc chamber made with currentlyavailable polycrystalline type alumina material. The flux treatmentapparently not only provides a smoother exterior surface havingincreased in-line transmission, but also increases the total opticaltransmission by removing a surface layer from the material. The endresult is that lamps utilizing the improved polycrystalline aluminamaterial of the present invention exhibit increased lumen per wattvalues to provide a more efficient light source.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic view of a jacketed high pressure sodium vapor lampembodying the present invention;

FIG. 2 is a photograph at 200 times magnification illustratingunpolished polycrystalline alumina;

FIG. 3 is a photograph taken at the same magnification level of polishedpolycrystalline alumina material according to the present invention; and

FIG. 4 is a sectional view of the electrode configuration for the lampdepicted in FIG. 1.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

A high intensity sodium vapor discharge lamp in which the invention maybe embodied is illustrated at 1 in FIG. 1 and comprises an outervitreous envelope or jacket 2 of elongated ovoid shape. The neck 3 ofthe jacket is closed by a re-entrant stem 4 having a press 5 throughwhich extends stiff inlead wires 6 and 7 which are connected at theirouter ends to the threaded shell 8 and center contact 9 of aconventional screw base.

The inner envelope or arc tube 11 is made of sintered high densitypolycrystalline alumina ceramic as described in the aforementioned U.S.Pat. No. 3,026,210 which has had the major surfaces chemically treatedin accordance with the present invention to provide increased opticaltransmission by means more fully explained hereinafter. The ends of thetube are closed by thimble-like niobium metal end caps 12 and 13 whichhave been hermetically sealed to the alumina arc tube by means of aglassy sealing composition which is shown exaggerated in thickness at 14in FIG. 4.

Thermionic electrodes 15 are mounted on the ends of the arc tube. Asbest seen in FIG. 4, the electrode comprises an inner tungsten wire coil16 which is wound over a tungsten shank 17 crimped or welded in the endof a niobium tube 18 welded to the end cap. The central turns in theinner coil 16 are spread apart and the outer tungsten wire coil 19 isscrewed over the inner coil. A suitable electron-emissive mix may beapplied to the electrode coils by painting or alternatively by dippingthe coils in the suspension. The material is retained primarily in theinterstices between the turns of outer and inner coil and of inner coiland shank.

Lower tube 18 is pierced through at 21 and is used as an exhaust tubeduring manufacture of the lamp. After the gas filling and sodium mercuryamalgam has been introduced into the arc tube, exhaust tube 18 ishermetically pinched off by a cold weld indicated at 22 and servesthereafter as a reservoir for condensed sodium mercury amalgam. Uppertube 18' has no opening in the arc tube and is used to contain a smallamount of yttrium metal (not shown) which serves as a getter; the end ofthe tube is closed by a pinch 23 which forms a hermetic seal. Theillustrated lamp is limited to base down operation wherein the longerexhaust tube 18, which must be the coolest portion of the arc tube forthe amalgam to condense therein, is located lowermost.

The arc tube is supported within the outer envelope by means of a mountcomprising a single rod 25 which extends the length of the envelope frominlead 7 at the stem end to a dimple 26 at the dome end to which it isanchored by a resilient clamp 27. End cap 13 of the arc tube isconnected to the frame by band 29 while end cap 12 is connected toinlead 6 through band 30 and support rod 31. The inter-envelope space isdesirably evacuated in order to conserve heat; this is done prior tosealing off the outer jacket. A getter, suitably barium-aluminum alloypowder pressed into channeled rings 32, is flashed after sealing inorder to assure a high vacuum. A method of manufacturing this type lampconstruction is further disclosed in aforementioned U.S. Pat. 3,708,710,hence need not be repeated in connection with the present invention.

Basically, the present chemical polishing method comprises physicallycontacting the major surfaces of a light transmissive body ofpolycrystalline alumina (i.e., the arc tube 11 prior to assembly of thelamp 1) with a molten inorganic flux that dissolves alumina at amoderate rate until the surface layer of said major surfaces has beendissolved to provide a relatively smooth appearance. It is important incarrying out this type of chemical polishing treatment that the fluxcomposition also be selected so as to preferentially dissolve thesurface layer of the alumina grains or particles rather than dissolveany material at the grain boundaries. It can be noted from a visualinspection of the treated alumina surface shown in FIG. 3 of theaccompanying drawings as compared with an untreated surface shown inFIG. 2 that surface material is removed by the fluxing agent to providea leveling or flattening action which reduces the high spots on theindividual alumina particles without materially introducing low spots atthe grain boundaries. From these photographs taken with reflected light,it can also be observed that the untreated surface in FIG. 2 gives theappearance of a "dark" field because of the large amount of light beingscattered. The selection of particular flux compositions providing thispreferential dissolving action can be made routinely by visiblyinspecting the effect produced upon the treated alumina surfaces with aselected flux material which should remain stable in the moltencondition at elevated temperatures of treatment up to around 1000°C. Atmore elevated temperatures, it has been observed that undesirable grainboundary etching can take place with the preferred sodium borate fluxcompositions and which further depends upon the time of contact.

Useful fluxing agents to provide a relatively smooth and flat surface inthe foregoing manner should also not produce insoluble reaction productsat the molten liquid interface which hinder the dissolving process orform an optical scattering surface having poor in-line transmission. Thealkali metal salts provide a general class of useful flux compositionsdemonstrating the aforesaid thermal and chemical stability in a moltenstate. That class includes the alkali metal borates such as sodiumborate and potassium borate, along with other type binary oxide systemshaving an alkali metal oxide constituent. Ternary oxide systems mightalso provide the desired uniform and moderate dissolving action althoughrequiring more elevated temperatures to achieve a molten state thanrequired for the preferred alkali metal borates. Thus, while it ispreferred to carry out the dissolving action in air by immersing apolycrystalline body in the molten alkali metal borate bath atmoderately elevated temperatures not exceeding approximately 1000°C soas not to encounter excessive volatilization of this fluxing agent, itis contemplated that more elevated temperatures or still other operatingconditions can be employed because of the refractory nature ofpolycrystalline alumina. Employment of an alkali metal borate flux alsoproduces a glassy coating upon the treated alumina body requiringsubsequent removal for improved in-line transmission. The coating can bedissolved by washing the treated member in a dilute acid solution afterit has been removed from the molten flux bath and cooled. It is alsodesirable to minimize thermal shock when the treated member is firstremoved from the molten flux bath which can be provided in conventionalfashion by controlled cooling to ambient temperatures.

A specific example of the preferred treatment process according to thepresent invention, wherein an alkali metal borate compound is employedas a fluxing agent, will be given. A number of polycrystalline aluminatube samples were immersed in a sodium borate melt for various timeperiods at elevated temperatures in the range from about 762°C to 857°Cto measure the effect upon total optical transmission of the chemicalpolishing treatment. A eutectic composition of the sodium borate saltwas employed which can be represented by the general chemical formulaNa₂ O.2.28B₂ O₃, although it has been found that other compositionshaving a molar ratio range up to four moles B₂ O₃ per 1 mole Na₂ O canbe used without significantly affecting the desired results. Time andtemperature conditions were varied during treatment in this manner andthe in-line transmission improvements obtained thereby are reported intabular form below. The optical transmission measurements were conductedover the visible light spectrum with a Beckman model DBspectrophotometer using a method described in the above referenced U.S.Pat. No. 3,026,210 patent and the average values obtained at differenttreatment conditions are listed in Table I below.

                  TABLE I                                                         ______________________________________                                        Temperature                                                                              Time      Transmission Increase                                    (°C)                                                                              (Min.)    (%)                                                      ______________________________________                                        900        10        60                                                       "          5         50                                                       "          2         57                                                       850        10        58                                                       "          5         55                                                       "          2         52                                                       800        10        57                                                       "          5         57                                                       "          2         53                                                       750        10        15                                                       "          5         36                                                       "          2          10.5                                                    ______________________________________                                    

It will be apparent from the above optical transmission results that asubstantial improvement is obtained compared with unpolished aluminatubes and more improvement takes place at longer times and highertemperatures. On the other hand, it should be kept in mind thatpreferential etching at the grain boundaries has been experienced withthis fluxing agent when the treatment temperature exceeds approximately1000°C. It was also necessary before conducting the above reportedoptical measurements to remove a vitreous coating on the treatedsurfaces which had been produced by the molten fluxing action. Thetreated arc chambers were washed in a dilute mineral acid solution todissolve this coating after having been allowed to cool under ambientconditions following their removal from the molten flux bath.

A number of 400-watt size high pressure sodium vapor lamps utilizing theconstruction previously described were produced with the flux polishedarc chambers for comparison with lamps having arc chambers of unpolishedpolycrystalline alumina. An average 117.7-lumens-per-watt output wasobtained by conventional measurement upon 28 lamps constructed with theunpolished arc chambers. In comparison therewith, an average120.5-lumens-per-watt output was obtained upon 14 lamps fabricated withthe flux polished arc chambers which represents a measurable improvementattributable to the present invention.

It will be apparent from the foregoing description that variousmodifications can be employed to obtain the benefits of the presentinvention. For example, various modifications can be made in thechemical polishing treatment with comparable results such as byconducting the polishing in a neutral atmosphere rather than air.Likewise, different processing steps can be employed to remove residualcoatings adhering to the major surfaces of the polycrystalline aluminabody after contact with the molten flux than above described. It isintended to limit the present invention, therefore, only to the scope ofthe following claims.

What we claim and desire to secure by Letters Patent of the UnitedStates is:
 1. An improved high intensity electric discharge lampcomprising a light transmissive envelope having electrodes sealed intoits ends and containing an ionizable medium for carrying the discharge,wherein the improvement comprises utilizing as the light transmissiveenvelope a tube consisting essentially of high density, polycrystallinealumina having the major exterior surfaces flux polished so as to reducethe high spots on the individual exterior alumina crystals withoutmaterially etching grain boundaries and thereby to obtain increasedoptical transmission upon flux removal.
 2. An electric discharge lamp asin claim 1 wherein the ionizable medium comprises a filling of sodium,mercury, and an inert gas within said envelope.
 3. An electric dischargelamp as in claim 1 wherein the electrodes are coated with electronemission material.
 4. An electric discharge lamp as in claim 1 whereinpolycrystalline alumina comprises high purity alumina having an in-linetransmission of not less than 0.5% per millimeter thickness of said tubefor radiant energy of all wavelengths in the wavelength range from about0.3 micron to about 6.6 microns and having an in-line transmission ofnot less than 10% at some wavelength within said wavelength range.
 5. Anelectric discharge lamp as in claim 4 wherein the polycrystallinealumina comprises high purity alumina containing a small but effectiveamount up to 0.5 weight percent magnesia.
 6. An electric discharge lampas in claim 5 wherein the magnesia content is present primarily as analumina-magnesia spinel.